Senior CRA home-based Paris

ICON Strategic Solutions; France; Hybrid; EUR 50.000 - 70.000; Vollzeit

Benefits dieser Stelle

Various annual leave entitlements

Health insurance offerings

Competitive retirement planning

Global Employee Assistance Programme

Flexible optional benefits

Zusammenfassung

ICON Strategic Solutions is hiring a Senior Clinical Research Associate in France. This role involves overseeing clinical trial activities, ensuring compliance with regulations, and managing multiple sites. Ideal candidates will have a Bachelor’s degree in a relevant field and extensive experience in clinical research.

The position offers competitive salary and various benefits, prioritizing well-being and work-life balance. If you have strong communication skills and a commitment to excellence, we encourage you to apply for this fulfilling opportunity.

Qualifikationen

• Extensive experience as a Clinical Research Associate, strong understanding of clinical trial processes.
• Proven ability to manage multiple sites and projects simultaneously.
• Willingness to travel approximately 60%.

Aufgaben

• Monitoring clinical trial sites to ensure adherence to protocols and regulatory requirements.
• Conducting site visits to assess performance and resolve issues.
• Collaborating with teams to ensure accurate data collection.
• Providing training and guidance to site staff and CRAs.
• Building relationships with site personnel for smooth trial operations.

Kenntnisse

Clinical trial monitoring

Organizational skills

Problem-solving skills

Excellent communication

Stakeholder management

Ausbildung

Bachelor’s degree in a relevant scientific discipline

Tools

Clinical trial software

Jobbeschreibung

Paris Home‑Based Senior CRA Role

ICON plc is a world‑leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.

As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards.

What You Will Do

You will lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality and continuous improvement.

Key Responsibilities

• Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
• Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.
• Collaborating with cross‑functional teams to ensure timely and accurate data collection and reporting.
• Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.
• Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.

Your Profile

You will have a strong foundation in clinical trial monitoring, with the experience to work independently and guide others.

Required Qualifications And Experience

• Bachelor’s degree in a relevant scientific discipline or healthcare‑related field.
• Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements.
• Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem‑solving skills.
• Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools.
• Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment.
• Willingness to travel as required (approximately 60%).

What ICON Can Offer You

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits designed to be competitive within each country and focused on well‑being and work‑life balance opportunities for you and your family.

Our Benefits Examples Include

• Various annual leave entitlements.
• A range of health insurance offerings to suit you and your family’s needs.
• Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
• Global Employee Assistance Programme, LifeWorks, offering 24‑hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well‑being.
• Life assurance.
• Flexible country‑specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.

At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here.